Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACATGCAGAGAAGGAACGACTCC[A/G]AGAAGCACAACGCGCCGCCACACAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611730 | ||||||||||||||||||||
Literature Links: |
EPB41L5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
EPB41L5 - erythrocyte membrane protein band 4.1 like 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184937.1 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | NP_001171866.1 | |
NM_020909.3 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | NP_065960.2 | |
XM_006712651.1 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | XP_006712714.1 | |
XM_006712652.1 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | XP_006712715.1 | |
XM_006712653.1 | 262 | UTR 5 | XP_006712716.1 | |||
XM_011511529.2 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | XP_011509831.1 | |
XM_017004567.1 | 262 | Missense Mutation | CAA,CGA | Q,R 24 | XP_016860056.1 | |
XM_017004568.1 | 262 | UTR 5 | XP_016860057.1 |